Canonical Allele Identifier: CA913178150
Gene:

Linked Data

ClinVar Variation Id: 689913
ClinVar RCV Id: RCV000850765
dbSNP Id: rs1603219459

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.4437C>T , J01415.2:m.4437C>T GRCh38